dc.contributor.author |
Gunasekera, J.M.A. |
|
dc.contributor.author |
Jayasekera, G. A. U. |
|
dc.contributor.author |
Fernandopulle, N. D. |
|
dc.contributor.author |
Perera, K. L. N. |
|
dc.contributor.author |
De Silva, A. D. |
|
dc.date.accessioned |
2011-11-15T10:33:56Z |
|
dc.date.available |
2011-11-15T10:33:56Z |
|
dc.date.issued |
2010 |
|
dc.identifier.citation |
Annual Research Proceedings, University of Colombo held on 12th and 13th May 2010 |
en_US |
dc.identifier.uri |
http://archive.cmb.ac.lk:8080/xmlui/handle/70130/381 |
|
dc.description.abstract |
Recent developments in plant cell biology and molecular biology have provided a
powerful and novel means to supplement as well as complement the traditional breeding
methods of crop improvement. The transgenic approach of plant genetic engineering
provides access to an unlimited gene pool for the transfer of desirable genes between any
two species of interest, irrespective of their evolutionary or taxonomic relationship.
In order to develop transgenic insect resistant rice plants, techniques to develop an
efficient methodology to transform explants cells of rice and to regenerate intact rice
plants from local rice varieties were initially attempted.
Three Sri Lankan rice varieties (Bg 350, Bg 94-1 and Bg 352) were selected. Scutellum
derived calli induced on NB callus induction medium was chosen as the source of explants
cells for transformation and regeneration of rice plants. Calli were transformed with
Agrobacterium tumefaciens strain LBA 4404 harboring plasmid construct pCAMBIA
1301 containing GUS ($ Glucuronidase) gene as the reporter gene and hygromycin
resistance gene as the selectable marker gene placed under the CaMV 35 S promoter and
NOS terminator. Following co cultivation for 2 days calli were cultured in callus induction
medium (without hygromycin) for 2 weeks followed by with hygromycin (30 mg/L) for
another 2 – 4 weeks. Afterwards, calli were transferred to shoot regeneration medium and
rooting medium. Recovered intact plants were acclimatized in green house under
contained environment conditions.
Transgene integration to the rice genome was confirmed through PCR analysis. Overall
efficiency of obtaining transgenic rice from local rice varieties was determined to be
nearly 20%.
Developed and optimized methodology led to the introduction of Cry 1C and 2A genes
encoding insecticidal proteins from Bacillus thuringiensis to Bg 94-1. Insect bioassays
performed indicated insecticidal activity against Rice Leaffolder. This result taken
together with the above stated results illustrate the potential of this technology for
breeding effective insect resistance in Sri Lankan rice varieties |
|
dc.language.iso |
en |
en_US |
dc.publisher |
University of Colombo |
en_US |
dc.title |
Development of transgenic plants for Leaffolder (Cnaphalocrosis medinalis) resistance in local rice varieties |
en_US |
dc.type |
Research abstract |
en_US |